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Fatty-acid metabolism disorder / Hepatology / Hypoglycemia / Mitochondrial trifunctional protein deficiency / Carnitine / Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency / Newborn screening / Adipose tissue / Carnitine-acylcarnitine translocase deficiency / Health / Medicine / Rare diseases
Date: 2009-02-19 11:31:59
Fatty-acid metabolism disorder
Hepatology
Hypoglycemia
Mitochondrial trifunctional protein deficiency
Carnitine
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Newborn screening
Adipose tissue
Carnitine-acylcarnitine translocase deficiency
Health
Medicine
Rare diseases

NEWBORN SCREENING FACT SHEET LCHADD (Long Chain 3-Hydroxyacyl-CoA Dehydrogenese Deficiency) What is it? LCHADD stands for long chain 3-hydroxyacylCoA dehydrogenase deficiency. It is one type of fatty acid oxidation disor

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